The food and drug Administration abstract this paper aims to discuss the way the U.S Food and administration department makes it rules and how the agency implements them. It also presents an analysis of the enforcement process in the United States and given a way forward on the improvements in the enforcement of the law. Introduction body background of the food and drug administration. How the FDA makes it rules types of rules How the agency implements the rules Analysis of enforcement process f) conclusion background The food and Drug Administration is a scientific agency of the U.S.
Department of healthy and humans services that oversees the regulation of food products, human and animal drugs, medical devices and radiation among other public health products. FDA was established in 1906 to establish a foundation that would foster comprehensive, and science- based protections that ensure the highest quality of products essential for health and survival in America. The department grew from a single chemist in the U.S.
Departments of agriculture and eventually became attached to the Department of health and human services, as FDA in 1953. The agency boots of an administrative capacity of about 9,100 employees within and outside of the Washington D.C. 1 On its work-list are chemists, pharmacologist, physicians,microbiologists, veterinarians, pharmacists, and lawyers, among others. How the FDA makes it rules FDA is a regulatory agency like many others in the U.S. As an agency it is empowered to create and enforce rules and regulations that carry the full force of a law.
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